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TGGTTGGCTGTAAGGTTTTGGCATA[C/T]GGTGAATACCAGTCCCTTTCAAACA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
9 submissions
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Phenotype: |
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Literature Links: |
PLD5 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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PLD5 - phospholipase D family member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001195811.1 | 1718 | Silent Mutation | CCA,CCG | P,P 435 | NP_001182740.1 | |
NM_001195812.1 | 1718 | Silent Mutation | CCA,CCG | P,P 289 | NP_001182741.1 | |
NM_001320272.1 | 1718 | Silent Mutation | CCA,CCG | P,P 405 | NP_001307201.1 | |
NM_152666.2 | 1718 | Silent Mutation | CCA,CCG | P,P 497 | NP_689879.2 | |
XM_006711752.2 | 1718 | Silent Mutation | CCA,CCG | P,P 497 | XP_006711815.1 | |
XM_011544115.2 | 1718 | Silent Mutation | CCA,CCG | P,P 406 | XP_011542417.1 | |
XM_011544116.2 | 1718 | Silent Mutation | CCA,CCG | P,P 406 | XP_011542418.1 | |
XM_011544119.2 | 1718 | Silent Mutation | CCA,CCG | P,P 362 | XP_011542421.2 | |
XM_011544120.2 | 1718 | Silent Mutation | CCA,CCG | P,P 289 | XP_011542422.1 | |
XM_011544121.2 | 1718 | Silent Mutation | CCA,CCG | P,P 289 | XP_011542423.1 | |
XM_011544122.2 | 1718 | Silent Mutation | CCA,CCG | P,P 289 | XP_011542424.1 | |
XM_017000567.1 | 1718 | Silent Mutation | CCA,CCG | P,P 405 | XP_016856056.1 | |
XM_017000568.1 | 1718 | Silent Mutation | CCA,CCG | P,P 405 | XP_016856057.1 | |
XM_017000569.1 | 1718 | Silent Mutation | CCA,CCG | P,P 289 | XP_016856058.1 | |
XM_017000570.1 | 1718 | Silent Mutation | CCA,CCG | P,P 289 | XP_016856059.1 |